Other mutations in this stock |
Total: 106 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aatk |
A |
T |
11: 119,901,940 (GRCm39) |
S819T |
probably damaging |
Het |
Abca13 |
A |
T |
11: 9,241,698 (GRCm39) |
D1187V |
probably damaging |
Het |
Ak9 |
C |
A |
10: 41,300,623 (GRCm39) |
T1611K |
unknown |
Het |
Als2 |
G |
T |
1: 59,242,189 (GRCm39) |
T622K |
probably benign |
Het |
Ankrd40 |
G |
A |
11: 94,225,262 (GRCm39) |
A98T |
probably benign |
Het |
Ap1b1 |
T |
C |
11: 4,973,174 (GRCm39) |
L339P |
probably damaging |
Het |
Appl1 |
A |
C |
14: 26,669,084 (GRCm39) |
H363Q |
probably benign |
Het |
Atf6 |
T |
C |
1: 170,622,245 (GRCm39) |
N459D |
probably damaging |
Het |
Ccdc6 |
A |
T |
10: 70,024,993 (GRCm39) |
Q432L |
unknown |
Het |
Ccl21a |
T |
A |
4: 42,773,486 (GRCm39) |
Q84L |
probably damaging |
Het |
Cct4 |
A |
G |
11: 22,951,389 (GRCm39) |
I348V |
probably benign |
Het |
Cd300ld2 |
A |
G |
11: 114,904,550 (GRCm39) |
Y106H |
probably damaging |
Het |
Cdh19 |
C |
T |
1: 110,876,947 (GRCm39) |
E131K |
probably damaging |
Het |
Cdon |
A |
G |
9: 35,403,175 (GRCm39) |
D1095G |
probably damaging |
Het |
Cep85l |
T |
A |
10: 53,157,670 (GRCm39) |
R678* |
probably null |
Het |
Chst3 |
T |
A |
10: 60,021,465 (GRCm39) |
S461C |
probably damaging |
Het |
Clk1 |
A |
G |
1: 58,459,312 (GRCm39) |
I149T |
possibly damaging |
Het |
Clvs2 |
T |
A |
10: 33,389,301 (GRCm39) |
D313V |
possibly damaging |
Het |
Dap3 |
T |
C |
3: 88,840,913 (GRCm39) |
T75A |
probably benign |
Het |
Dnaaf1 |
T |
A |
8: 120,324,392 (GRCm39) |
F631L |
probably benign |
Het |
Dnah14 |
A |
T |
1: 181,597,325 (GRCm39) |
N3549I |
probably benign |
Het |
Dnah17 |
A |
T |
11: 117,931,870 (GRCm39) |
Y3701N |
probably damaging |
Het |
Dock6 |
A |
G |
9: 21,752,796 (GRCm39) |
V339A |
possibly damaging |
Het |
Dpp6 |
T |
A |
5: 27,803,832 (GRCm39) |
C259* |
probably null |
Het |
Dqx1 |
A |
G |
6: 83,036,024 (GRCm39) |
T119A |
probably benign |
Het |
Dync1h1 |
G |
T |
12: 110,583,310 (GRCm39) |
R469L |
probably benign |
Het |
Eno4 |
C |
T |
19: 58,951,260 (GRCm39) |
A424V |
probably benign |
Het |
Entrep1 |
A |
T |
19: 23,972,221 (GRCm39) |
I161N |
possibly damaging |
Het |
Fads1 |
T |
A |
19: 10,163,162 (GRCm39) |
D146E |
probably damaging |
Het |
Fam171a1 |
C |
T |
2: 3,224,543 (GRCm39) |
T303M |
probably damaging |
Het |
Fbxw20 |
C |
T |
9: 109,050,423 (GRCm39) |
D401N |
probably benign |
Het |
Fcho1 |
T |
A |
8: 72,163,068 (GRCm39) |
T654S |
possibly damaging |
Het |
Flad1 |
C |
A |
3: 89,315,858 (GRCm39) |
E235* |
probably null |
Het |
Flrt2 |
G |
T |
12: 95,745,907 (GRCm39) |
A82S |
probably benign |
Het |
Gabrg3 |
A |
T |
7: 56,829,386 (GRCm39) |
S124T |
probably benign |
Het |
Galt |
C |
T |
4: 41,756,777 (GRCm39) |
T139I |
probably benign |
Het |
Garin4 |
A |
G |
1: 190,895,153 (GRCm39) |
S497P |
probably damaging |
Het |
Gfod1 |
T |
C |
13: 43,456,861 (GRCm39) |
E38G |
possibly damaging |
Het |
Gm10330 |
A |
G |
12: 23,829,992 (GRCm39) |
I63T |
possibly damaging |
Het |
Gm49359 |
A |
G |
13: 62,602,867 (GRCm39) |
V111A |
probably benign |
Het |
Gpank1 |
C |
T |
17: 35,340,734 (GRCm39) |
|
probably benign |
Het |
Hck |
T |
C |
2: 152,973,185 (GRCm39) |
L156P |
probably damaging |
Het |
Hcn3 |
G |
T |
3: 89,057,267 (GRCm39) |
R444S |
probably damaging |
Het |
Hephl1 |
T |
C |
9: 14,988,236 (GRCm39) |
N624S |
probably damaging |
Het |
Hmcn1 |
A |
G |
1: 150,632,309 (GRCm39) |
I876T |
probably damaging |
Het |
Ifi207 |
CTGTTGATGAAGTTGCATGTGGAGCCAGGAGGTTGCTAGATGTTGTTGATAGAGTTGCATGTGGAGCCAGGAGGTTGCTAGATGTTGTTGATAGAGTTGCATGTGGAGCCAGGAGGTTGCTAGATGCTGTTGATACAGTTGCTTGTGGAGCCAGGAGGTTGCTAGATGCTGTTGATAGAGTTGCATATGGAGCCAGGAGGATGCTATATGTTGTTGATGAAGTTGCATGTGGAGCCAGGAG |
CTGTTGATAGAGTTGCATGTGGAGCCAGGAGGTTGCTAGATGTTGTTGATAGAGTTGCATGTGGAGCCAGGAGGTTGCTAGATGCTGTTGATACAGTTGCTTGTGGAGCCAGGAGGTTGCTAGATGCTGTTGATAGAGTTGCATATGGAGCCAGGAGGATGCTATATGTTGTTGATGAAGTTGCATGTGGAGCCAGGAG |
1: 173,556,762 (GRCm39) |
|
probably benign |
Het |
Itga9 |
T |
A |
9: 118,500,859 (GRCm39) |
D377E |
possibly damaging |
Het |
Itprid1 |
G |
T |
6: 55,944,051 (GRCm39) |
R417L |
probably benign |
Het |
Klk1b11 |
C |
T |
7: 43,425,954 (GRCm39) |
L32F |
probably benign |
Het |
Lta4h |
A |
G |
10: 93,310,412 (GRCm39) |
S427G |
probably benign |
Het |
Lxn |
T |
A |
3: 67,368,651 (GRCm39) |
I122F |
probably damaging |
Het |
Lyz1 |
A |
G |
10: 117,124,492 (GRCm39) |
V148A |
possibly damaging |
Het |
Mael |
G |
T |
1: 166,032,424 (GRCm39) |
Q326K |
probably benign |
Het |
Magi3 |
T |
C |
3: 103,923,264 (GRCm39) |
D1151G |
possibly damaging |
Het |
Map3k9 |
C |
A |
12: 81,769,261 (GRCm39) |
G929V |
probably benign |
Het |
Mcoln1 |
A |
G |
8: 3,555,771 (GRCm39) |
Y22C |
probably damaging |
Het |
Mier3 |
G |
T |
13: 111,827,870 (GRCm39) |
M45I |
probably benign |
Het |
Mrpl1 |
T |
C |
5: 96,371,746 (GRCm39) |
V91A |
probably damaging |
Het |
Myo7a |
T |
C |
7: 97,740,281 (GRCm39) |
H571R |
probably benign |
Het |
Myom1 |
T |
A |
17: 71,374,325 (GRCm39) |
W601R |
probably damaging |
Het |
Myom3 |
C |
T |
4: 135,505,479 (GRCm39) |
T456I |
probably benign |
Het |
Nags |
A |
T |
11: 102,037,584 (GRCm39) |
H225L |
probably benign |
Het |
Ncaph |
C |
A |
2: 126,958,554 (GRCm39) |
K488N |
probably damaging |
Het |
Nkain3 |
C |
T |
4: 20,484,897 (GRCm39) |
R60H |
probably damaging |
Het |
Nlrp9a |
A |
T |
7: 26,261,944 (GRCm39) |
M698L |
probably benign |
Het |
Nmur2 |
A |
C |
11: 55,931,308 (GRCm39) |
I134M |
probably benign |
Het |
Nrp2 |
A |
C |
1: 62,784,670 (GRCm39) |
E273A |
probably benign |
Het |
Nup85 |
A |
G |
11: 115,468,787 (GRCm39) |
D210G |
possibly damaging |
Het |
Obscn |
A |
G |
11: 59,006,643 (GRCm39) |
F1173S |
probably damaging |
Het |
Or5ac24 |
A |
T |
16: 59,165,145 (GRCm39) |
C306* |
probably null |
Het |
Otogl |
T |
A |
10: 107,652,974 (GRCm39) |
E1126V |
probably null |
Het |
Pfkl |
T |
C |
10: 77,833,426 (GRCm39) |
I259V |
probably benign |
Het |
Phkg1 |
A |
T |
5: 129,893,863 (GRCm39) |
Y291N |
probably benign |
Het |
Piezo2 |
T |
G |
18: 63,163,450 (GRCm39) |
H2156P |
probably damaging |
Het |
Piezo2 |
C |
A |
18: 63,208,790 (GRCm39) |
V1408L |
probably damaging |
Het |
Pira13 |
T |
A |
7: 3,819,997 (GRCm39) |
E640V |
unknown |
Het |
Plekhg3 |
A |
G |
12: 76,622,694 (GRCm39) |
T646A |
probably benign |
Het |
Plk5 |
C |
G |
10: 80,193,830 (GRCm39) |
R40G |
probably damaging |
Het |
Ppp1r12a |
T |
C |
10: 108,098,224 (GRCm39) |
S838P |
probably damaging |
Het |
Rarb |
A |
T |
14: 16,435,235 (GRCm38) |
Y270* |
probably null |
Het |
Rbm15 |
T |
C |
3: 107,239,312 (GRCm39) |
E362G |
possibly damaging |
Het |
Rcan1 |
A |
G |
16: 92,262,741 (GRCm39) |
F76L |
|
Het |
Rdh19 |
T |
C |
10: 127,696,142 (GRCm39) |
L298P |
probably damaging |
Het |
Rims1 |
T |
A |
1: 22,498,773 (GRCm39) |
H57L |
|
Het |
Rlf |
T |
C |
4: 121,004,751 (GRCm39) |
T1520A |
probably benign |
Het |
Rnase1 |
T |
A |
14: 51,382,964 (GRCm39) |
H130L |
possibly damaging |
Het |
Samd8 |
T |
A |
14: 21,842,569 (GRCm39) |
M360K |
probably damaging |
Het |
Samhd1 |
A |
G |
2: 156,956,205 (GRCm39) |
L329P |
probably damaging |
Het |
Scube1 |
C |
T |
15: 83,494,394 (GRCm39) |
E878K |
probably damaging |
Het |
Sema3b |
T |
C |
9: 107,476,154 (GRCm39) |
Y689C |
probably damaging |
Het |
Semp2l2a |
T |
C |
8: 13,886,697 (GRCm39) |
T465A |
possibly damaging |
Het |
Sh3pxd2b |
A |
T |
11: 32,373,361 (GRCm39) |
N843Y |
possibly damaging |
Het |
Slco1a6 |
C |
T |
6: 142,035,575 (GRCm39) |
C583Y |
probably damaging |
Het |
Smg1 |
A |
C |
7: 117,811,786 (GRCm39) |
V88G |
unknown |
Het |
Spata24 |
T |
A |
18: 35,790,054 (GRCm39) |
N146Y |
probably damaging |
Het |
Tcf3 |
C |
A |
10: 80,253,191 (GRCm39) |
V258L |
probably benign |
Het |
Tiam2 |
T |
C |
17: 3,465,011 (GRCm39) |
Y247H |
probably damaging |
Het |
Ticrr |
T |
C |
7: 79,310,604 (GRCm39) |
F173L |
possibly damaging |
Het |
Tpp2 |
A |
G |
1: 43,993,811 (GRCm39) |
E232G |
probably damaging |
Het |
Trank1 |
T |
A |
9: 111,174,547 (GRCm39) |
V138E |
probably damaging |
Het |
Ttll3 |
T |
C |
6: 113,369,596 (GRCm39) |
S47P |
probably benign |
Het |
Utp4 |
C |
T |
8: 107,632,857 (GRCm39) |
T280M |
probably damaging |
Het |
Vmn1r123 |
A |
T |
7: 20,896,794 (GRCm39) |
N229Y |
probably benign |
Het |
Vmn1r85 |
A |
T |
7: 12,818,942 (GRCm39) |
Y67* |
probably null |
Het |
Zbtb12 |
T |
A |
17: 35,114,320 (GRCm39) |
V35E |
possibly damaging |
Het |
Zmym6 |
T |
A |
4: 127,017,854 (GRCm39) |
F1212I |
probably damaging |
Het |
|
Other mutations in Itpr3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00715:Itpr3
|
APN |
17 |
27,302,603 (GRCm39) |
missense |
probably benign |
0.05 |
IGL00980:Itpr3
|
APN |
17 |
27,329,930 (GRCm39) |
missense |
probably benign |
|
IGL01151:Itpr3
|
APN |
17 |
27,310,503 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01289:Itpr3
|
APN |
17 |
27,318,739 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01403:Itpr3
|
APN |
17 |
27,337,569 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01666:Itpr3
|
APN |
17 |
27,336,152 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01897:Itpr3
|
APN |
17 |
27,330,236 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02003:Itpr3
|
APN |
17 |
27,340,449 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02012:Itpr3
|
APN |
17 |
27,323,069 (GRCm39) |
missense |
probably benign |
|
IGL02063:Itpr3
|
APN |
17 |
27,338,997 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02146:Itpr3
|
APN |
17 |
27,336,249 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02158:Itpr3
|
APN |
17 |
27,317,416 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02177:Itpr3
|
APN |
17 |
27,318,588 (GRCm39) |
missense |
possibly damaging |
0.74 |
IGL02247:Itpr3
|
APN |
17 |
27,317,153 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02606:Itpr3
|
APN |
17 |
27,333,486 (GRCm39) |
splice site |
probably benign |
|
IGL02651:Itpr3
|
APN |
17 |
27,325,372 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02902:Itpr3
|
APN |
17 |
27,323,530 (GRCm39) |
missense |
probably benign |
0.21 |
IGL03001:Itpr3
|
APN |
17 |
27,308,586 (GRCm39) |
splice site |
probably benign |
|
IGL03004:Itpr3
|
APN |
17 |
27,316,952 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL03065:Itpr3
|
APN |
17 |
27,310,907 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03117:Itpr3
|
APN |
17 |
27,338,240 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03181:Itpr3
|
APN |
17 |
27,330,242 (GRCm39) |
missense |
probably benign |
|
IGL03404:Itpr3
|
APN |
17 |
27,310,492 (GRCm39) |
missense |
probably damaging |
1.00 |
Allure
|
UTSW |
17 |
27,326,277 (GRCm39) |
missense |
probably damaging |
1.00 |
alopecia
|
UTSW |
17 |
27,314,452 (GRCm39) |
missense |
probably damaging |
0.98 |
Beauty
|
UTSW |
17 |
27,325,316 (GRCm39) |
missense |
probably damaging |
1.00 |
Opuesto
|
UTSW |
17 |
27,306,566 (GRCm39) |
missense |
probably damaging |
1.00 |
Paradox
|
UTSW |
17 |
27,317,145 (GRCm39) |
missense |
probably damaging |
1.00 |
Pulchritude
|
UTSW |
17 |
27,305,934 (GRCm39) |
missense |
probably damaging |
0.97 |
R0010:Itpr3
|
UTSW |
17 |
27,339,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R0055:Itpr3
|
UTSW |
17 |
27,317,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R0068:Itpr3
|
UTSW |
17 |
27,323,034 (GRCm39) |
splice site |
probably benign |
|
R0068:Itpr3
|
UTSW |
17 |
27,323,034 (GRCm39) |
splice site |
probably benign |
|
R0104:Itpr3
|
UTSW |
17 |
27,314,966 (GRCm39) |
missense |
probably benign |
0.01 |
R0195:Itpr3
|
UTSW |
17 |
27,333,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R0212:Itpr3
|
UTSW |
17 |
27,308,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R0454:Itpr3
|
UTSW |
17 |
27,332,793 (GRCm39) |
missense |
probably benign |
|
R0485:Itpr3
|
UTSW |
17 |
27,330,903 (GRCm39) |
missense |
probably damaging |
0.98 |
R0501:Itpr3
|
UTSW |
17 |
27,326,263 (GRCm39) |
missense |
probably benign |
0.09 |
R0781:Itpr3
|
UTSW |
17 |
27,329,529 (GRCm39) |
missense |
probably benign |
0.00 |
R0890:Itpr3
|
UTSW |
17 |
27,307,985 (GRCm39) |
nonsense |
probably null |
|
R1028:Itpr3
|
UTSW |
17 |
27,310,343 (GRCm39) |
missense |
probably benign |
0.04 |
R1144:Itpr3
|
UTSW |
17 |
27,333,897 (GRCm39) |
missense |
probably benign |
0.01 |
R1347:Itpr3
|
UTSW |
17 |
27,330,535 (GRCm39) |
missense |
probably benign |
0.02 |
R1347:Itpr3
|
UTSW |
17 |
27,330,535 (GRCm39) |
missense |
probably benign |
0.02 |
R1458:Itpr3
|
UTSW |
17 |
27,337,346 (GRCm39) |
missense |
probably benign |
0.01 |
R1463:Itpr3
|
UTSW |
17 |
27,336,128 (GRCm39) |
splice site |
probably benign |
|
R1472:Itpr3
|
UTSW |
17 |
27,333,199 (GRCm39) |
missense |
probably benign |
0.09 |
R1529:Itpr3
|
UTSW |
17 |
27,324,459 (GRCm39) |
splice site |
probably null |
|
R1533:Itpr3
|
UTSW |
17 |
27,314,534 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1537:Itpr3
|
UTSW |
17 |
27,333,121 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1618:Itpr3
|
UTSW |
17 |
27,335,581 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1672:Itpr3
|
UTSW |
17 |
27,307,987 (GRCm39) |
missense |
probably benign |
|
R1726:Itpr3
|
UTSW |
17 |
27,330,664 (GRCm39) |
missense |
probably damaging |
0.96 |
R1865:Itpr3
|
UTSW |
17 |
27,338,997 (GRCm39) |
missense |
probably benign |
0.01 |
R1940:Itpr3
|
UTSW |
17 |
27,330,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R2023:Itpr3
|
UTSW |
17 |
27,321,785 (GRCm39) |
missense |
possibly damaging |
0.76 |
R2063:Itpr3
|
UTSW |
17 |
27,317,050 (GRCm39) |
missense |
probably benign |
0.19 |
R2064:Itpr3
|
UTSW |
17 |
27,317,050 (GRCm39) |
missense |
probably benign |
0.19 |
R2065:Itpr3
|
UTSW |
17 |
27,317,050 (GRCm39) |
missense |
probably benign |
0.19 |
R2067:Itpr3
|
UTSW |
17 |
27,317,050 (GRCm39) |
missense |
probably benign |
0.19 |
R2068:Itpr3
|
UTSW |
17 |
27,317,050 (GRCm39) |
missense |
probably benign |
0.19 |
R2219:Itpr3
|
UTSW |
17 |
27,334,027 (GRCm39) |
missense |
probably benign |
|
R2248:Itpr3
|
UTSW |
17 |
27,334,033 (GRCm39) |
missense |
probably damaging |
1.00 |
R2291:Itpr3
|
UTSW |
17 |
27,332,553 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2320:Itpr3
|
UTSW |
17 |
27,314,889 (GRCm39) |
missense |
probably benign |
|
R2864:Itpr3
|
UTSW |
17 |
27,310,525 (GRCm39) |
missense |
probably benign |
0.01 |
R2865:Itpr3
|
UTSW |
17 |
27,310,525 (GRCm39) |
missense |
probably benign |
0.01 |
R3778:Itpr3
|
UTSW |
17 |
27,314,446 (GRCm39) |
missense |
possibly damaging |
0.57 |
R3881:Itpr3
|
UTSW |
17 |
27,332,814 (GRCm39) |
missense |
probably benign |
0.01 |
R3979:Itpr3
|
UTSW |
17 |
27,310,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R3979:Itpr3
|
UTSW |
17 |
27,304,105 (GRCm39) |
missense |
probably benign |
0.23 |
R4224:Itpr3
|
UTSW |
17 |
27,326,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R4259:Itpr3
|
UTSW |
17 |
27,325,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R4321:Itpr3
|
UTSW |
17 |
27,330,948 (GRCm39) |
missense |
probably benign |
0.00 |
R4466:Itpr3
|
UTSW |
17 |
27,325,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R4493:Itpr3
|
UTSW |
17 |
27,323,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R4597:Itpr3
|
UTSW |
17 |
27,312,257 (GRCm39) |
missense |
probably damaging |
1.00 |
R4823:Itpr3
|
UTSW |
17 |
27,304,121 (GRCm39) |
missense |
probably benign |
0.30 |
R4921:Itpr3
|
UTSW |
17 |
27,316,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R4974:Itpr3
|
UTSW |
17 |
27,302,582 (GRCm39) |
missense |
probably damaging |
0.96 |
R5063:Itpr3
|
UTSW |
17 |
27,308,885 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5079:Itpr3
|
UTSW |
17 |
27,317,397 (GRCm39) |
missense |
probably damaging |
1.00 |
R5303:Itpr3
|
UTSW |
17 |
27,335,663 (GRCm39) |
missense |
probably benign |
0.38 |
R5518:Itpr3
|
UTSW |
17 |
27,306,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R5521:Itpr3
|
UTSW |
17 |
27,326,308 (GRCm39) |
missense |
probably benign |
0.09 |
R5566:Itpr3
|
UTSW |
17 |
27,334,926 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5567:Itpr3
|
UTSW |
17 |
27,322,880 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5579:Itpr3
|
UTSW |
17 |
27,332,493 (GRCm39) |
missense |
probably damaging |
1.00 |
R5610:Itpr3
|
UTSW |
17 |
27,337,540 (GRCm39) |
missense |
probably benign |
0.42 |
R5658:Itpr3
|
UTSW |
17 |
27,326,852 (GRCm39) |
missense |
possibly damaging |
0.74 |
R5856:Itpr3
|
UTSW |
17 |
27,325,379 (GRCm39) |
missense |
probably damaging |
1.00 |
R5872:Itpr3
|
UTSW |
17 |
27,305,950 (GRCm39) |
missense |
probably benign |
0.02 |
R5878:Itpr3
|
UTSW |
17 |
27,329,836 (GRCm39) |
missense |
probably benign |
0.01 |
R5889:Itpr3
|
UTSW |
17 |
27,334,039 (GRCm39) |
missense |
probably damaging |
0.99 |
R5907:Itpr3
|
UTSW |
17 |
27,336,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R5930:Itpr3
|
UTSW |
17 |
27,329,895 (GRCm39) |
missense |
possibly damaging |
0.49 |
R5987:Itpr3
|
UTSW |
17 |
27,323,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R6029:Itpr3
|
UTSW |
17 |
27,317,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R6195:Itpr3
|
UTSW |
17 |
27,305,934 (GRCm39) |
missense |
probably damaging |
0.97 |
R6213:Itpr3
|
UTSW |
17 |
27,330,174 (GRCm39) |
missense |
probably benign |
0.03 |
R6233:Itpr3
|
UTSW |
17 |
27,305,934 (GRCm39) |
missense |
probably damaging |
0.97 |
R6376:Itpr3
|
UTSW |
17 |
27,314,449 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6514:Itpr3
|
UTSW |
17 |
27,310,344 (GRCm39) |
missense |
probably benign |
|
R6515:Itpr3
|
UTSW |
17 |
27,310,344 (GRCm39) |
missense |
probably benign |
|
R6516:Itpr3
|
UTSW |
17 |
27,310,344 (GRCm39) |
missense |
probably benign |
|
R6955:Itpr3
|
UTSW |
17 |
27,340,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R7002:Itpr3
|
UTSW |
17 |
27,329,554 (GRCm39) |
missense |
probably benign |
0.00 |
R7064:Itpr3
|
UTSW |
17 |
27,308,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R7257:Itpr3
|
UTSW |
17 |
27,337,535 (GRCm39) |
missense |
probably benign |
0.00 |
R7349:Itpr3
|
UTSW |
17 |
27,326,786 (GRCm39) |
splice site |
probably null |
|
R7469:Itpr3
|
UTSW |
17 |
27,340,028 (GRCm39) |
missense |
possibly damaging |
0.74 |
R7493:Itpr3
|
UTSW |
17 |
27,313,774 (GRCm39) |
missense |
probably benign |
0.09 |
R7510:Itpr3
|
UTSW |
17 |
27,308,013 (GRCm39) |
missense |
probably damaging |
0.97 |
R7565:Itpr3
|
UTSW |
17 |
27,329,862 (GRCm39) |
missense |
probably benign |
0.01 |
R7616:Itpr3
|
UTSW |
17 |
27,307,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R7728:Itpr3
|
UTSW |
17 |
27,317,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R7779:Itpr3
|
UTSW |
17 |
27,315,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R7788:Itpr3
|
UTSW |
17 |
27,337,571 (GRCm39) |
nonsense |
probably null |
|
R7871:Itpr3
|
UTSW |
17 |
27,336,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R7889:Itpr3
|
UTSW |
17 |
27,335,751 (GRCm39) |
missense |
probably damaging |
1.00 |
R7966:Itpr3
|
UTSW |
17 |
27,331,002 (GRCm39) |
critical splice donor site |
probably null |
|
R8065:Itpr3
|
UTSW |
17 |
27,329,836 (GRCm39) |
missense |
probably benign |
0.01 |
R8067:Itpr3
|
UTSW |
17 |
27,329,836 (GRCm39) |
missense |
probably benign |
0.01 |
R8230:Itpr3
|
UTSW |
17 |
27,326,711 (GRCm39) |
critical splice donor site |
probably null |
|
R8263:Itpr3
|
UTSW |
17 |
27,334,887 (GRCm39) |
nonsense |
probably null |
|
R8264:Itpr3
|
UTSW |
17 |
27,323,086 (GRCm39) |
synonymous |
silent |
|
R8269:Itpr3
|
UTSW |
17 |
27,312,258 (GRCm39) |
missense |
possibly damaging |
0.60 |
R8271:Itpr3
|
UTSW |
17 |
27,306,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R8316:Itpr3
|
UTSW |
17 |
27,325,199 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8354:Itpr3
|
UTSW |
17 |
27,334,893 (GRCm39) |
missense |
possibly damaging |
0.74 |
R8413:Itpr3
|
UTSW |
17 |
27,330,900 (GRCm39) |
missense |
probably damaging |
1.00 |
R8437:Itpr3
|
UTSW |
17 |
27,326,277 (GRCm39) |
missense |
probably damaging |
1.00 |
R8676:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R8679:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R8846:Itpr3
|
UTSW |
17 |
27,330,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R8884:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R8885:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R8886:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R8887:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R8888:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R8891:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R8896:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R8975:Itpr3
|
UTSW |
17 |
27,335,628 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9025:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R9026:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R9063:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R9087:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R9088:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R9089:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R9091:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R9200:Itpr3
|
UTSW |
17 |
27,326,636 (GRCm39) |
missense |
probably damaging |
0.99 |
R9270:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R9271:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R9294:Itpr3
|
UTSW |
17 |
27,330,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R9389:Itpr3
|
UTSW |
17 |
27,314,899 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9433:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R9434:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R9443:Itpr3
|
UTSW |
17 |
27,324,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R9472:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R9474:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R9475:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R9476:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R9477:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R9507:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R9508:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R9511:Itpr3
|
UTSW |
17 |
27,337,651 (GRCm39) |
unclassified |
probably benign |
|
R9694:Itpr3
|
UTSW |
17 |
27,334,927 (GRCm39) |
missense |
probably damaging |
0.99 |
R9789:Itpr3
|
UTSW |
17 |
27,308,915 (GRCm39) |
missense |
probably benign |
0.15 |
V7732:Itpr3
|
UTSW |
17 |
27,330,000 (GRCm39) |
splice site |
probably null |
|
V7732:Itpr3
|
UTSW |
17 |
27,329,998 (GRCm39) |
splice site |
probably benign |
|
Z1088:Itpr3
|
UTSW |
17 |
27,332,502 (GRCm39) |
missense |
possibly damaging |
0.50 |
Z1177:Itpr3
|
UTSW |
17 |
27,338,961 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Itpr3
|
UTSW |
17 |
27,333,903 (GRCm39) |
missense |
probably damaging |
1.00 |
Z31818:Itpr3
|
UTSW |
17 |
27,314,452 (GRCm39) |
missense |
probably damaging |
0.98 |
|